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49540-21-8

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49540-21-8 Usage

Description

Butanamide, 2-hydroxy-4-(methylthio)-, also known as 2-hydroxy-4-(methylthio)butanamide, is a chemical compound with the molecular formula C5H11NO2S. It is a derivative of butanamide, featuring a hydroxy group and a methylthio group attached to the 2nd and 4th carbon of the butanamide chain, respectively. Butanamide, 2-hydroxy-4-(methylthio)is known for its potential biological and pharmacological activities, including antimicrobial and antioxidant properties, and is commonly used as an intermediate in organic synthesis and pharmaceutical manufacturing.

Uses

Used in Organic Synthesis:
Butanamide, 2-hydroxy-4-(methylthio)is used as an intermediate in organic synthesis for the production of various chemical compounds and materials. Its unique structure allows for further functionalization and modification, making it a versatile building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Manufacturing:
Butanamide, 2-hydroxy-4-(methylthio)is utilized in the pharmaceutical industry as a key intermediate in the synthesis of drugs and active pharmaceutical ingredients. Its presence in the molecular structure can contribute to the desired biological activity and pharmacological properties of the final drug product.
Used in Antimicrobial Applications:
Butanamide, 2-hydroxy-4-(methylthio)has been studied for its antimicrobial properties, making it a potential candidate for use in the development of new antimicrobial agents. Its ability to inhibit the growth of harmful microorganisms can be leveraged in various applications, such as in the formulation of antimicrobial coatings, disinfectants, and preservatives.
Used in Antioxidant Applications:
Due to its antioxidant properties, Butanamide, 2-hydroxy-4-(methylthio)can be used in the development of antioxidants for various industries, including food, cosmetics, and pharmaceuticals. Its ability to neutralize free radicals and protect against oxidative damage can help extend the shelf life of products and maintain their quality.
Used in Drug Development and Therapeutic Applications:
As a compound with potential biological and pharmacological activities, Butanamide, 2-hydroxy-4-(methylthio)is a promising candidate for further research in drug development. Its unique structure and properties can be explored for the development of new therapeutic agents targeting various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 49540-21-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,4 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 49540-21:
(7*4)+(6*9)+(5*5)+(4*4)+(3*0)+(2*2)+(1*1)=128
128 % 10 = 8
So 49540-21-8 is a valid CAS Registry Number.

49540-21-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-4-methylsulfanylbutanamide

1.2 Other means of identification

Product number -
Other names 2-hydroxy-4-methylsulfanyl-butyric acid amide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:49540-21-8 SDS

49540-21-8Relevant articles and documents

Process for the preparation of hydroxymethylbutyric acid

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Page column 5-8, (2008/06/13)

The invention relates to a new process for the preparation of hydroxymethylthiobutyric acid by sulphuric hydrolysis of hydroxymethylthiobutyronitrile.

Process for producing 2-hydroxy-4-methylthiobutanoic acid

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, (2008/06/13)

Methyl 2-hydroxy-4-methylthiobutanoate and formamide are produced by means of reacting 2-hydroxy-4-methylthiobutanamide obtained by hydration of 2-hydroxy-4-methylthiobutyronitrile with methyl formate. Said methyl 2-hydroxy-4-methylthiobutanoate is hydrolyzed to give 2-hydroxy-4-methylthiobutanoic acid and methanol. No sulfuric acid is employed as a reacting agent, hence exhaustion of a large quantity of ammonium sulfate is prevented. Formamide and methanol thus produced can be recycled as reactants.

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